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Antibody Against Periostin, and a Pharmaceutical Composition comprising it for Preventing or Treating a Disease in which Periostin is Involved

a technology of periostin and anti-cell adhesive properties, which is applied in the field of anti-periostin, can solve the problems of affecting the vital prognosis unable to maintain the quality of life, and limited activities in the daily life of patients with heart failure, so as to improve the long-term vital prognosis and improve the quality of life

Active Publication Date: 2009-03-19
OSAKA UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0019]The present invention aims to provide, e.g., a novel and effective prophylactic or therapeutic agent for heart failure, which enables an improvement in the quality of life and an improvement in long-term vital prognosis. More specifically, the present invention aims to provide an antibody against a periostin isoform having anti-cell adhesive activity, specifically recognizing a site responsible for anti-cell adhesion. The present invention also aims to provide a hybridoma producing the antibody, a method for producing the hybridoma, and a method for producing the antibody by culturing the hybridoma. The present invention further aims to provide a pharmaceutical composition comprising the antibody for preventing or treating a disease in which a periostin isoform having anti-cell adhesive activity is involved. The present invention further aims to provide a method for preventing or treating a disease in which a periostin isoform having anti-cell adhesive activity is involved, comprising administering the pharmaceutical composition to a patient, as well as a method for diagnosing the disease.
[0031]Based on these findings, the inventors of the present invention deduced that the cell detachment effect (i.e., cell-releasing effect) of PN-1 protein is related to the release of cancer cells from their primary tumor during the cancer metastasis processes mentioned above, and thereby facilitates cancer metastasis. Thus, they attempted to clarify the relationship between PN-1 protein and the pathology of cancer.
[0038]Further, analysis of periostin splice variants highly expressed during the pathology of cancer revealed that PN-1 having the functions of inhibiting cell adhesion and separating adhered cells is expressed at very high level in tumor tissues of model mice for lung metastasis of mouse melanoma B16-F10 cells or mouse 4T1 breast cancer cells when compared to normal tissues, thus showing that PN-1 is expressed at a very high level during the pathology of cancer.
[0044]Furthermore, the inventors of the present invention prepared a monoclonal antibody against the human periostin Exon-17 peptide chain (hereinafter referred to as “anti-Exon-17 monoclonal antibody”). In experiments using model mice for lung metastasis of mouse melanoma B16-F10 cells, administration of the anti-Exon-17 monoclonal antibody showed cancer growth inhibition and inhibitory effects on the metastasis rate and the number of metastasized colonies from primary tumor to lung.

Problems solved by technology

However, these drugs have been shown to impair vital prognosis during long-term administration, due to excessive consumption of myocardial energy.
However, patients with heart failure have limited activities in their daily life and cannot maintain their quality of life because they are prohibited from hard exercise or the like.
Moreover, the vital prognosis of patients with heart failure cannot be fully ensured.
However, on a worldwide basis, the cancer mortality rate continues to increase for reasons such as aging population, and cancer remains the primary cause of death.
This is because not a few patients will die of cancer metastasis even when primary carcinoma removal is completely achieved, and there is a limit to surgical operation, radiation therapy or chemotherapy for completely blocking cancer metastasis, so that the distant metastasis of cancer is still directly or indirectly related to the cause of cancer death.
However, there has been neither a report of antibodies showing the structure of a region responsible for cell adhesive activity of periostin nor a report showing the relation between the cell adhesive activity of periostin and diseases such as heart failure.

Method used

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  • Antibody Against Periostin, and a Pharmaceutical Composition comprising it for Preventing or Treating a Disease in which Periostin is Involved
  • Antibody Against Periostin, and a Pharmaceutical Composition comprising it for Preventing or Treating a Disease in which Periostin is Involved
  • Antibody Against Periostin, and a Pharmaceutical Composition comprising it for Preventing or Treating a Disease in which Periostin is Involved

Examples

Experimental program
Comparison scheme
Effect test

preparation example 1

Search for Periostin by Subtraction

[0166]1-1 Preparation of Pathologic Model Rats of Heart Failure and Collection of Left Ventricular Samples

[0167]Male Dahl salt-sensitive rats (Dahl-S) (Shimizu Laboratory Supplies) were raised on an 8% high salt diet from 6 weeks of age, and the left ventricle was collected from three animals each at cardiac hypertrophy stage (11 weeks of age) and heart failure stage (14 weeks of age).

[0168]1-2 Preparation of mRNA

[0169]Total RNA was prepared from about 500 mg of the left ventricle using ISOGEN (Nippon Gene) as instructed by the manufacturer. Then, mRNA was purified from about 40 μg of the combined total RNA from three animals each at cardiac hypertrophy stage and heart failure stage using Fast Track 2.0 Kit (Invitrogen) as instructed by the manufacturer to recover about 3 μg of mRNA at each stage.

[0170]1-3 cDNA Subtraction

[0171]cDNA subtraction was performed using PCR-Select cDNA subtraction kit (Clontech) as instructed by the manufacturer. That is...

preparation example 2

Cloning of Rat Periostin cDNA

[0182]Rat periostin cDNA was isolated by screening 10 phage subpools of about 4000 clones (a total of about 40,000 clones) prepared from a rat aorta cDNA library (Clontech) inserted into λgt11 vector by PCR using primers (1) 5′-GTTCATTGAAGGTGGCGATGGTC-3′ (SEQ ID NO: 15), and (2) 5′-GAGATAAAATCCCTGCATGGTCCT-3′ (SEQ ID NO: 16) designed on the basis of the nucleotide sequence of SF014 to give 3 positive subpools. One of the subpools was screened by hybridization using the fragment amplified by PCR as a probe labeled with alkaline phosphatase using AlkPhos Direct™ (Amersham Pharmacia) to give one positive clone rat periostin #1. Its insert fragment was subcloned into the EcoRI site of pBluescript II (Stratagene) and the total nucleotide sequence was determined according to the method of Preparation example 1-5.

[0183]The resulting clone had a length of about 3 kb corresponding to nucleotide 292 to the 3′ end of mouse periostin (GenBank Accession No. D13664), ...

preparation example 3

Construction of a Myc-His-rat Periostin Fusion Protein Expression Vector

[0187]An expression vector having a Myc epitope and 6 histidine tags at the carboxyl terminus of the protein translated from the coding region of the rat periostin gene obtained in Preparation example 2, and having a CMV promoter, was prepared.

[0188]Initially, a fragment of about 500 bp obtained by digestion of rat periostin 5′RACE #1 obtained in Preparation example 2 with restriction enzymes EcoRI and HindIII and a fragment of about 2780 bp obtained by digestion of rat periostin #1 obtained in Preparation example 2 with restriction enzymes HindIII and HpaI were ligated to a vector fragment obtained by digesting pTracer-CMV2 vector (Invitrogen) with restriction enzymes EcoRI and EcoRV using a ligation kit (Takara Bio Inc.) to give a plasmid designated as pTracer-CMV2 / rat periostin. Thus prepared pTracer-CMV2 / rat periostin was digested with restriction enzymes EcoRI and SmaI to give a fragment of about 2330 bp co...

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Abstract

The present invention provides an antibody against a periostin isoform having anti-cell adhesive activity, especially an anti-periostin antibody having the ability to neutralize anti-cell adhesive properties, as well as a prophylactic or therapeutic agent for periostin-related diseases comprising the antibody. The present invention also provides methods for detecting and quantifying the periostin isoform in a sample by using the antibody, as well as a method for diagnosing periostin-related diseases comprising measuring the amount of the periostin isoform by the detection or quantification method.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application is a continuation-in-part of International Patent Application No. PCT / JP2006 / 326280, filed Dec. 28, 2006, which claims priority to Japan 380009 / 2005, filed Dec. 28, 2005, Japan 169494 / 2007, filed Jun. 27, 2007, JP 33827 / 2008, Feb. 14, 2008, the disclosures of each of which are hereby incorporated by reference.BACKGROUND OF THE INVENTION[0002](i) Field of the Invention:[0003]The present invention relates to antibodies against periostin isoforms having anti-cell adhesive properties, especially anti-periostin antibodies having the ability to neutralize anti-cell adhesive properties. More specifically, it relates to anti-periostin antibodies specifically recognizing a site responsible for anti-cell adhesion of periostin having anti-cell adhesive properties specifically expressed in interstitial tissue during tissue restructuring such as cardiac hypertrophy, which are useful for prevention or treatment of periostin-related dis...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K39/395C07K16/00G01N33/68A61P25/00A61P1/18A61P31/12A61P35/00A61P11/00A61P9/00C12N5/00
CPCA61K2039/505C07K2317/73C07K16/18A61P1/18A61P11/00A61P25/00A61P31/12A61P35/00A61P9/00
Inventor TANIYAMA, YOSHIAKIMORISHITA, RYUICHIKATSURAGI, NARUTO
Owner OSAKA UNIV
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